ENST00000359526.9:c.1398A>T
MANE Select
|
ENSP00000352516.3:p.Glu466Asp
|
|
ENST00000676604.1:n.1010A>T
|
|
|
ENST00000676610.1:c.1350A>T
|
ENSP00000504236.1:p.Glu450Asp
|
|
ENST00000676820.1:n.1406A>T
|
|
|
ENST00000676868.1:n.2034A>T
|
|
|
ENST00000677013.1:c.*1040A>T
|
ENSP00000503135.1:n.*1040A>T
|
|
ENST00000677250.1:c.*470A>T
|
ENSP00000502894.1:n.*470A>T
|
|
ENST00000677616.1:c.1041A>T
|
ENSP00000503055.1:p.Glu347Asp
|
|
ENST00000677634.1:c.1350A>T
|
ENSP00000504246.1:p.Glu450Asp
|
|
ENST00000677685.1:c.*575A>T
|
ENSP00000503407.1:n.*575A>T
|
|
ENST00000677783.1:n.1820A>T
|
|
|
ENST00000677946.1:c.1350A>T
|
ENSP00000504202.1:p.Glu450Asp
|
|
ENST00000678024.1:n.1493A>T
|
|
|
ENST00000678694.1:n.671A>T
|
|
|
ENST00000678804.1:c.1350A>T
|
ENSP00000503853.1:p.Glu450Asp
|
|
ENST00000679103.1:c.1350A>T
|
ENSP00000503151.1:p.Glu450Asp
|
|
ENST00000679313.1:c.1350A>T
|
ENSP00000504512.1:p.Glu450Asp
|
|
ENST00000340748.8:c.1350A>T
|
ENSP00000345739.3:p.Glu450Asp
|
|
ENST00000359526.8:c.1398A>T
|
ENSP00000352516.3:p.Glu466Asp
|
|
ENST00000540357.5:c.342A>T
|
ENSP00000440457.2:p.Glu114Asp
|
|
ENST00000585843.1:n.555A>T
|
|
|
ENST00000592705.5:c.*1088A>T
|
ENSP00000466657.1:n.*1088A>T
|
|
NM_001130823.1:c.1398A>T , LRG_362t1:c.1398A>T
|
NP_001124295.1:p.Glu466Asp
|
|
NM_001379.2:c.1350A>T
|
NP_001370.1:p.Glu450Asp
|
|
XM_011527772.1:c.1398A>T
|
XP_011526074.1:p.Glu466Asp
|
|
XM_011527773.1:c.1350A>T
|
XP_011526075.1:p.Glu450Asp
|
|
XM_011527774.1:c.987A>T
|
XP_011526076.1:p.Glu329Asp
|
|
NM_001130823.2:c.1398A>T
|
NP_001124295.1:p.Glu466Asp
|
|
NM_001318730.1:c.1350A>T
|
NP_001305659.1:p.Glu450Asp
|
|
NM_001318731.1:c.1035A>T
|
NP_001305660.1:p.Glu345Asp
|
|
NM_001379.3:c.1350A>T
|
NP_001370.1:p.Glu450Asp
|
|
NM_001130823.3:c.1398A>T
MANE Select
|
NP_001124295.1:p.Glu466Asp
|
|
NM_001318730.2:c.1350A>T
|
NP_001305659.1:p.Glu450Asp
|
|
NM_001318731.2:c.1035A>T
|
NP_001305660.1:p.Glu345Asp
|
|
NM_001379.4:c.1350A>T
|
NP_001370.1:p.Glu450Asp
|
|